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Journal Abstract Search

592 related items for PubMed ID: 18371543

  • 1. Complement factor H deficiency and posttransplantation glomerulonephritis with isolated C3 deposits.
    Boyer O, Noël LH, Balzamo E, Guest G, Biebuyck N, Charbit M, Salomon R, Frémeaux-Bacchi V, Niaudet P.
    Am J Kidney Dis; 2008 Apr; 51(4):671-7. PubMed ID: 18371543
    [Abstract] [Full Text] [Related]

  • 2. Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.
    Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B, Grünfeld JP, Lesavre P, Noël LH, Fakhouri F.
    J Med Genet; 2007 Mar; 44(3):193-9. PubMed ID: 17018561
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  • 3. Pulse cyclophosphamide therapy and clinical remission in atypical hemolytic uremic syndrome with anti-complement factor H autoantibodies.
    Boyer O, Balzamo E, Charbit M, Biebuyck-Gougé N, Salomon R, Dragon-Durey MA, Frémeaux-Bacchi V, Niaudet P.
    Am J Kidney Dis; 2010 May; 55(5):923-7. PubMed ID: 20202729
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  • 4. Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation.
    Schejbel L, Schmidt IM, Kirchhoff M, Andersen CB, Marquart HV, Zipfel P, Garred P.
    Genes Immun; 2011 Mar; 12(2):90-9. PubMed ID: 21270828
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  • 5. Mouse podocyte complement factor H: the functional analog to human complement receptor 1.
    Alexander JJ, Wang Y, Chang A, Jacob A, Minto AW, Karmegam M, Haas M, Quigg RJ.
    J Am Soc Nephrol; 2007 Apr; 18(4):1157-66. PubMed ID: 17344423
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  • 6. Hemolytic uremic syndrome recurrence after renal transplantation.
    Loirat C, Fremeaux-Bacchi V.
    Pediatr Transplant; 2008 Sep; 12(6):619-29. PubMed ID: 18482212
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  • 7. Haemolytic uraemic syndrome caused by factor H mutation: is single kidney transplantation under intensive plasmatherapy an option?
    Hirt-Minkowski P, Schaub S, Mayr M, Schifferli JA, Dickenmann M, Frémeaux-Bacchi V, Steiger J.
    Nephrol Dial Transplant; 2009 Nov; 24(11):3548-51. PubMed ID: 19633317
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  • 8. A favorable 3-year outcome of kidney transplantation in atypical hemolytic uremic syndrome associated with a factor H mutation: case report.
    Albertazzi V, Bonucchi D, De Amicis S, Americo C, Ghiandai G, Cappelli G.
    Transplant Proc; 2010 May; 42(4):1352-4. PubMed ID: 20534299
    [Abstract] [Full Text] [Related]

  • 9. Heterogeneous pattern of renal disease associated with homozygous factor H deficiency.
    Servais A, Noël LH, Dragon-Durey MA, Gübler MC, Rémy P, Buob D, Cordonnier C, Makdassi R, Jaber W, Boulanger E, Lesavre P, Frémeaux-Bacchi V.
    Hum Pathol; 2011 Sep; 42(9):1305-11. PubMed ID: 21396679
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  • 12. Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H.
    Pickering MC, Cook HT, Warren J, Bygrave AE, Moss J, Walport MJ, Botto M.
    Nat Genet; 2002 Aug; 31(4):424-8. PubMed ID: 12091909
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  • 13. Atypical hemolytic uremic syndrome: update on the complement system and what is new.
    Hirt-Minkowski P, Dickenmann M, Schifferli JA.
    Nephron Clin Pract; 2010 Aug; 114(4):c219-35. PubMed ID: 20090363
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  • 15. Pathology of renal diseases associated with dysfunction of the alternative pathway of complement: C3 glomerulopathy and atypical hemolytic uremic syndrome (aHUS).
    Sethi S, Fervenza FC.
    Semin Thromb Hemost; 2014 Jun; 40(4):416-21. PubMed ID: 24799306
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  • 16. Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis.
    Licht C, Fremeaux-Bacchi V.
    Thromb Haemost; 2009 Feb; 101(2):271-8. PubMed ID: 19190809
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  • 18. C3 glomerulonephritis secondary to mutations in factors H and I: rapid recurrence in deceased donor kidney transplant effectively treated with eculizumab.
    Garg N, Zhang Y, Nicholson-Weller A, Khankin EV, Borsa NG, Meyer NC, McDermott S, Stillman IE, Rennke HG, Smith RJ, Pavlakis M.
    Nephrol Dial Transplant; 2018 Dec 01; 33(12):2260-2265. PubMed ID: 29370420
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  • 20. C3 glomerulonephritis associated with a missense mutation in the factor H gene.
    Sugimoto K, Fujita S, Miyazaki K, Okada M, Takemura T.
    Tohoku J Exp Med; 2012 Jul 01; 227(3):211-5. PubMed ID: 22790979
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